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Kaletra
Kaletra - 49349-024-21 - (Kaletra)
Drug Information of Kaletra
| Product NDC: | 49349-024 |
| Proprietary Name: | Kaletra |
| Non Proprietary Name: | Kaletra |
| Active Ingredient(s): | 200; 50 mg/1; mg/1 & nbsp; Kaletra |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kaletra
| Product NDC: | 49349-024 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075659 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100927 |
Package Information of Kaletra
| Package NDC: | 49349-024-21 |
| Package Description: | 120 TABLET in 1 CANISTER (49349-024-21) |
NDC Information of Kaletra
| NDC Code | 49349-024-21 |
| Proprietary Name | Kaletra |
| Package Description | 120 TABLET in 1 CANISTER (49349-024-21) |
| Product NDC | 49349-024 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Kaletra |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100927 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | LOPINAVIR; RITONAVIR |
| Strength Number | 200; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC],HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC] |
